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PATHOPHYSIOLOGY EXAM QUESTIONS AND ANSWERS

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PATHOPHYSIOLOGY EXAM QUESTIONS AND ANSWERS

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Pathophysiology
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Pathophysiology
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Pathophysiology

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Uploaded on
January 10, 2025
Number of pages
81
Written in
2024/2025
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PATHOPHYSIOLOGY EXAM 1 2024-2025

QUESTIONS AND ANSWERS.




An ordered photographic display of a set of chromosomes

from a single cell is a(n):

A) metaphase spread.

B) autosomal spread.

C) karyotype.

D) anaphase spread. - ANSWER -c



An error in which homologous chromosomes fail to separate

during meiosis is termed:

A) aneuploidy.

B) nondisjunction.

C) polyploidy.

,D) anaplasia. - ANSWER -b



A somatic cell that does not contain a multiple of 23

chromosomes is called:

A) an aneuploid cell.

B) a euploid cell.

C) a polyploidy cell.

D) a haploid cell. - ANSWER -a



A 20-year-old pregnant female gives birth to a stillborn child.

Autopsy reveals that the fetus has 92 chromosomes. Which

of the following describes this condition?

A) Euploidy

B) Triploidy

C) Tetraploidy

D) Aneuploidy - ANSWER -c



If a person is a chromosomal mosaic, the person may:

,A) be a carrier of the genetic disease.

B) have a mild form of the genetic disease.

C) have two genetic diseases.

D) be sterile as a result of the genetic disease. - ANSWER -b



The most common cause of Down syndrome is:

A) paternal nondisjunction.

B) maternal translocations.

C) maternal nondisjunction.

D) paternal translocations. - ANSWER -c



Risk factors for Down syndrome include:

A) fetal exposure to mutagens in the uterus.

B) increased paternal age.

C) family history of Down syndrome.

D) pregnancy in women over age 35. - ANSWER -d

, A 13-year-old girl has a karyotype that reveals an absent

homologous X chromosome with only a single X

chromosome present. Her condition is called:

A) Down syndrome.

B) Cri du chat syndrome.

C) Turner syndrome.

D) Edward syndrome - ANSWER -c



A child is diagnosed with cystic fibrosis. History reveals that

the child's parents are first cousins. Cystic fibrosis was most

likely the result of:

A) X inactivation.

B) genomic imprinting.

C) consanguinity.

D) obligate carriers. - ANSWER -c



Joey, age 9, is admitted to a pediatric unit with Duchenne

muscular dystrophy. He inherited this condition through a:

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